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Journal of the Neurological Sciences|July 25, 2006
Atypical language impairment in two siblings: relationship with electrical status epilepticus during slow wave sleepJulien Praline, Marie-Anne Barthez, Pierre Castelnau, et al.Epilepsia|July 21, 2011
Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutationsMathieu Milh, Nathalie Villeneuve, Mondher Chouchane, et al.Epileptic Disorders : International Epilepsy Journal with Videotape|March 29, 2006
Cognitive functions in children with benign childhood epilepsy with centrotemporal spikes (BECTS)Florence Pinton, Béatrice Ducot, Jacques Motte, et al.The Journal of Pediatrics|March 6, 2004
Endocrine involvement in pediatric-onset Langerhans' cell histiocytosis: a population-based studyJean Donadieu, Maria-Alejandra Rolon, Caroline Thomas, et al.Frontiers in Pediatrics|March 22, 2021
West Syndrome Is an Exceptional Presentation of Pyridoxine- and Pyridoxal Phosphate-Dependent Epilepsy: Data From a French Cohort and Review of the LiteratureMarc Gibaud, Magalie Barth, Jérémie Lefranc, et al.Epilepsia|July 3, 2013
Children often present with infantile spasms after herpetic encephalitisGemma Aznar Laín, Georges Dellatolas, Monika Eisermann, et al.Journal of Medical Genetics|June 5, 2010
Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndromeChristel Depienne, Oriane Trouillard, Isabelle Gourfinkel-An, et al.Neurology|March 4, 2020
Movement disorders in patients with alternating hemiplegia: "Soft" and "stiff" at the same timeEleni Panagiotakaki, Diane Doummar, Erika Nogue, et al.European Journal of Medical Genetics|September 18, 2020
A novel pathogenic variant in DYNC1H1 causes various upper and lower motor neuron anomaliesLouis M Viollet, Kathryn J Swoboda, Rong Mao, et al.Neurology. Genetics|December 25, 2019
Epilepsy with migrating focal seizures: KCNT1 mutation hotspots and phenotype variabilityGiulia Barcia, Nicole Chemaly, Mathieu Kuchenbuch, et al.Pageof 3